A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17143283



Internal ID21409385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:36363390..36363390hg38UCSC Ensembl
chr6:36331167..36331167hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg38102
hg19102
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5634535
Supporting Variants
SamplesHG00512
Known GenesETV7
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17143283
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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